Literature DB >> 3889143

Application of a unique monoclonal antibody as a marker for nonproliferating subpopulations of cells of some tissue.

E Wang, J G Krueger.   

Abstract

A monoclonal antibody (clone S-30), directed to a protein of 57,000 daltons, was developed from the fusion of mouse myeloma cells and the spleen cells of mice injected with cytoskeletal extracts of fibroblasts that have been aged in in vitro culturing conditions according to a schedule of serial passaging (Cristofalo VJ, Charpentier R: J Tissue Culture Meth 6:117, 1981; Wang E: J Cell Biol, submitted). The staining activity of S-30 antibody was observed exclusively in the nuclei of nonproliferating senescent fibroblasts, but not in their young counterparts. Immunolocalization of S-30 antibody in frozen tissues from various sites reveals the positive staining reaction in the nuclear envelope region in those cells that are at the final stage of differentiation and are no longer replicating. These tissue sites include epithelial cells of the suprabasal layer of epidermis, hair sheath, and tongue, a subpopulation of fibroblasts in the dermis, chondrocytes, hepatocytes, and cells of cardiac muscle. The absence of S-30 staining activity was noted in tissues such as simple epithelium located in the gastrointestinal tract and kidney, and keratinocytes in the basal layer. These results suggest that the S-30 antibody can be used as a marker for nonproliferating cells both in cultured fibroblasts and in some tissues. It seems that the mechanism that controls the cessation of cell proliferation is related, in part, to the postmitotic expression of the 57,000 dalton protein.

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Year:  1985        PMID: 3889143     DOI: 10.1177/33.6.3889143

Source DB:  PubMed          Journal:  J Histochem Cytochem        ISSN: 0022-1554            Impact factor:   2.479


  7 in total

1.  Absence of three secreted proteins and presence of a 57-kDa protein related to irreversible arrest of cell growth.

Authors:  G Ching; E Wang
Journal:  Proc Natl Acad Sci U S A       Date:  1988-01       Impact factor: 11.205

2.  Statin expression in the untreated and SarCNU-exposed human glioma cell line, SK-MG-1.

Authors:  H M Schipper; V Skalski; L C Panasci; E Wang
Journal:  Cancer Chemother Pharmacol       Date:  1990       Impact factor: 3.333

Review 3.  The assessment of cellular proliferation by immunohistochemistry: a review of currently available methods and their applications.

Authors:  C C Yu; A L Woods; D A Levison
Journal:  Histochem J       Date:  1992-03

4.  Nuclear phospholipids during the adaptation of human EUE cells to hypertonic stress.

Authors:  A Fraschini; A M Fuhrman Conti
Journal:  Histochem Cell Biol       Date:  1995-01       Impact factor: 4.304

5.  All-trans retinoic acid (ATRA)-induced apoptosis is preceded by G1 arrest in human MCF-7 breast cancer cells.

Authors:  R Mangiarotti; M Danova; R Alberici; C Pellicciari
Journal:  Br J Cancer       Date:  1998       Impact factor: 7.640

6.  Rapid disappearance of statin, a nonproliferating and senescent cell-specific protein, upon reentering the process of cell cycling.

Authors:  E Wang
Journal:  J Cell Biol       Date:  1985-11       Impact factor: 10.539

7.  Characterization of two populations of statin and the relationship of their syntheses to the state of cell proliferation.

Authors:  G Ching; E Wang
Journal:  J Cell Biol       Date:  1990-02       Impact factor: 10.539

  7 in total

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